Pannexin-1 Modulates Inhibitory Transmission and Hippocampal Synaptic Plasticity

Biomolecules. 2023 May 25;13(6):887. doi: 10.3390/biom13060887.

Abstract

Pannexin-1 (Panx1) hemichannel is a non-selective transmembrane channel that may play important roles in intercellular signaling by allowing the permeation of ions and metabolites, such as ATP. Although recent evidence shows that the Panx1 hemichannel is involved in controlling excitatory synaptic transmission, the role of Panx1 in inhibitory transmission remains unknown. Here, we studied the contribution of Panx1 to the GABAergic synaptic efficacy onto CA1 pyramidal neurons (PyNs) by using patch-clamp recordings and pharmacological approaches in wild-type and Panx1 knock-out (Panx1-KO) mice. We reported that blockage of the Panx1 hemichannel with the mimetic peptide 10Panx1 increases the synaptic level of endocannabinoids (eCB) and the activation of cannabinoid receptors type 1 (CB1Rs), which results in a decrease in hippocampal GABAergic efficacy, shifting excitation/inhibition (E/I) balance toward excitation and facilitating the induction of long-term potentiation. Our finding provides important insight unveiling that Panx1 can strongly influence the overall neuronal excitability and play a key role in shaping synaptic changes affecting the amplitude and direction of plasticity, as well as learning and memory processes.

Keywords: GABA transmission; endocannabinoids; excitatory/inhibitory balance; pannexin-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Connexins / genetics
  • Connexins / metabolism
  • Hippocampus* / metabolism
  • Long-Term Potentiation / physiology
  • Mice
  • Nerve Tissue Proteins* / genetics
  • Nerve Tissue Proteins* / metabolism
  • Neuronal Plasticity* / genetics
  • Neuronal Plasticity* / physiology
  • Pyramidal Cells* / metabolism
  • Pyramidal Cells* / physiology
  • Synaptic Transmission

Substances

  • Connexins
  • Nerve Tissue Proteins
  • Panx1 protein, mouse

Grants and funding

This research was funded by: FONDECYT 11150776 and 1201342 (Á.O.A.), 1171006 (M.F.), 1211045 (A.D.M.) FONDEF ID21I10153 (A.D.M.); Millennium Institute ICM-ANID ICN09–022 and ACE210014 (Á.O.A. and A.D.M.); Proyecto Puente UV 20993 and partial supports from DIUV-CI Grant No. 01/2006 (M.F., Universidad de Valparaíso); and ANID Doctoral Fellowship 21190247 (C.F.-M.), 21190642 (F.G.-R.), 21181214 (O.S.).